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PIcc Cost EffectiveneSS and Safety of Infusional Therapy (PrInCESS)

Primary Purpose

Thrombosis, Infection

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Peripherally inserted central catheter (PICC)
Central venous catheter
Sponsored by
Hospital de Clinicas de Porto Alegre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Thrombosis focused on measuring Central Venous Catheters, Vascular Access Devices, Nursing, Cost Effectiveness, PICC

Eligibility Criteria

5 Years - 80 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient above 5 years old,
  • Hospitalized,
  • With prescription of infusion therapy for 10 days or more of antibiotics, antineoplastics or other drugs with a pH lower than 5 or higher than 9 and / or osmolarity above 900 mOsm / l, parenteral nutrition or hypertonic solutions.

Exclusion Criteria:

  • Insertion of the central catheter in emergency situations.
  • Critical patient in the acute or terminal stage;
  • Chronic renal disease stage IV or V and indication of hemodialysis;
  • Pediatric patients with leukemia until the induction phase;
  • Adult patients diagnosed with acute myeloid leukemia;
  • Autologous and allogenic marrow transplantation;
  • Upper limb with anatomical alteration, presence of arteriovenous fistula, axillary emptying or previous vascular procedure;
  • Presence of skin changes in the area of the puncture, such as thrombophlebitis, dermatitis, cellulitis, burn among others;
  • Patient using crutches or devices that require exertion or support in the upper limbs.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Peripherally inserted central catheter

    Central venous catheter

    Arm Description

    The peripherally inserted central catheter (PICC) with 3 to 6 French calibers, with one, two or three lumens Groshong and PowerPICC models. These calibers are dependent on the amount of lumens, which are used for single or concomitant infusions.

    The central venous catheter (CVC), with a short stay of 3 to 7 French gauges with one or more lumens.

    Outcomes

    Primary Outcome Measures

    infectious complications
    bloodstream infection
    thrombotic complications
    radiographically-confirmed upper-extremity deep vein thrombosis
    mechanical complications
    chest X-ray
    accidental removal
    obstruction or accidental removal

    Secondary Outcome Measures

    Cost Effectiveness
    reduction of the rates composite outcome of complications Catheter occlusion: significant reduction of infusion flow or an impairment of blood back-flow; Catheter damage, malposition and catheter migration.

    Full Information

    First Posted
    January 2, 2018
    Last Updated
    January 2, 2018
    Sponsor
    Hospital de Clinicas de Porto Alegre
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03392831
    Brief Title
    PIcc Cost EffectiveneSS and Safety of Infusional Therapy
    Acronym
    PrInCESS
    Official Title
    Comparative Cost-Effectiveness and Safety of Infusional Therapy With Central Venous Catheters Versus Peripherally Inserted Central Catheters: a Randomized Clinical Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 2018 (Anticipated)
    Primary Completion Date
    December 2019 (Anticipated)
    Study Completion Date
    December 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Hospital de Clinicas de Porto Alegre

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Infusion therapy comprises the parenteral administration of solutions, through peripheral or central vascular access. Some solutions and drugs are highly irritating to the vascular endothelium and therefore cannot be administered in peripheral vessels, because increase the risk of phlebitis and/or tissue necrosis. Thus, the alternative is the central venous catheter (CVC) where the access can be by direct puncture of a central vessel or peripheral vessel puncture with progression of the catheter until central positioning, through a peripherally inserted central catheter (PICC). We must take into account that indication, insertion, handling and maintenance must be balanced with risks, benefits and costs. The insertion and maintenance of both catheters are not free of complications. Among the most frequent are: Infection, thrombosis, lumen occlusion and accidental early removal of the catheter. This often implies in the need for new vascular access, impacting on morbidity and increased treatment costs. The PICC has some advantages over CVC, for example: avoids repetitive punctures and consequently decreased handling/pain; a lower risk of infection; avoids the use of venous dissections; reduces the risks of pneumothorax/hemothorax; reduces the risk of infiltration, extravasation, necrosis tissue and chemical phlebitis. Further, the PICC can be used as a long-term catheter with easy handling in extra-hospital condition. All these advantages suggest that this technology offers lower cost to the health system and more benefits for patients. However, PICC is not available for use in infusion therapy in patients of the Brazilian public health system, except for neonates. The available literature does not address cost-effectiveness studies of this technology in the international scope comparing the PICC versus CVC. And, similarly, we do not have studies conducted in Brazil to incorporate this technology into our public health system, based on its benefits and potential cost reduction. In order to fill this gap, this study aims to test if the use of PICC in patients with infusional therapy equal or superior to 10 days (Intervention Group), will show a lower incidence in the outcomes (infection, thrombosis or mechanical complications), besides being more cost-effective when compared to the use of CVC of short stay (Control Group).
    Detailed Description
    Patient recruitment: Adult and pediatric patients will be included during hospitalization in the clinical/surgical units at the Hospital de Clínicas de Porto Alegre. Variables of registry: Clinical data (diagnosis, reason for indication of catheter, site of insertion, vessel size, pharmacological treatment); Socio-demographic (age, sex, education, income); Ultrasonography (vessel evaluation); Radiography (to ensure the correct positioning of the catheter); economic variables (costs of all inputs used). Data collection: All variables will be recorded in an instrument developed by the authors. Statistical analysis: Continuous variables will be described using means and standard deviations or median and range in case of asymmetric distribution of data. Categorical variables will be presented using frequency distribution. Analyses will be conducted using chi-square and t tests for independent samples. P values <0.05 will be considered statistically significant. A Statistical Package for Social Sciences v.20.0 will be used. The Cox Regression Analysis and Log-rank test will compare the groups in relation to complication-free survival. Cost-effectiveness analysis: The cost-effectiveness analysis will be measured by the incremental cost-effectiveness ratio (ICER), showed by the difference in cost between intervention and control group, divided by the difference in their effect. It represents the average incremental cost associated with 1 additional unit of the measure of effect. The cost-effectiveness analysis will be based on the cost estimate for insertion and maintenance of the catheter, including values of the inputs used, medicines, costs with professionals, surgical environment, laboratory and imaging exams.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Thrombosis, Infection
    Keywords
    Central Venous Catheters, Vascular Access Devices, Nursing, Cost Effectiveness, PICC

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Prospective Randomized Open Blinded End-Point (PROBE) study
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    624 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Peripherally inserted central catheter
    Arm Type
    Experimental
    Arm Description
    The peripherally inserted central catheter (PICC) with 3 to 6 French calibers, with one, two or three lumens Groshong and PowerPICC models. These calibers are dependent on the amount of lumens, which are used for single or concomitant infusions.
    Arm Title
    Central venous catheter
    Arm Type
    Active Comparator
    Arm Description
    The central venous catheter (CVC), with a short stay of 3 to 7 French gauges with one or more lumens.
    Intervention Type
    Other
    Intervention Name(s)
    Peripherally inserted central catheter (PICC)
    Intervention Description
    The peripherally inserted central catheter with different sizes (French scale). Trained vascular access nurses will perform the insertion of the PICC, guided by ultrasound at bedside using the Seldinger technique. A suitable sterile field will be established. In the case of children the procedure may be performed at the Ambulatory Surgical Center
    Intervention Type
    Other
    Intervention Name(s)
    Central venous catheter
    Intervention Description
    The central venous catheter with different sizes (French scale). Trained doctors will perform the insertion of the CVC, guided by ultrasound at bedside using the Seldinger technique. A suitable sterile field will be established.The decision of the caliber depends on the clinical evaluation and need for multiple infusional therapy.
    Primary Outcome Measure Information:
    Title
    infectious complications
    Description
    bloodstream infection
    Time Frame
    up to 30 days or the end of therapy
    Title
    thrombotic complications
    Description
    radiographically-confirmed upper-extremity deep vein thrombosis
    Time Frame
    up to 30 days or the end of therapy
    Title
    mechanical complications
    Description
    chest X-ray
    Time Frame
    up to 30 days or the end of therapy
    Title
    accidental removal
    Description
    obstruction or accidental removal
    Time Frame
    up to 30 days or need for another catheter
    Secondary Outcome Measure Information:
    Title
    Cost Effectiveness
    Description
    reduction of the rates composite outcome of complications Catheter occlusion: significant reduction of infusion flow or an impairment of blood back-flow; Catheter damage, malposition and catheter migration.
    Time Frame
    up to 30 days or the end of therapy

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    5 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patient above 5 years old, Hospitalized, With prescription of infusion therapy for 10 days or more of antibiotics, antineoplastics or other drugs with a pH lower than 5 or higher than 9 and / or osmolarity above 900 mOsm / l, parenteral nutrition or hypertonic solutions. Exclusion Criteria: Insertion of the central catheter in emergency situations. Critical patient in the acute or terminal stage; Chronic renal disease stage IV or V and indication of hemodialysis; Pediatric patients with leukemia until the induction phase; Adult patients diagnosed with acute myeloid leukemia; Autologous and allogenic marrow transplantation; Upper limb with anatomical alteration, presence of arteriovenous fistula, axillary emptying or previous vascular procedure; Presence of skin changes in the area of the puncture, such as thrombophlebitis, dermatitis, cellulitis, burn among others; Patient using crutches or devices that require exertion or support in the upper limbs.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Eneida R Rabelo da Silva
    Phone
    +5551 33085226
    Email
    eneidarabelo@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Simone S Fantin
    Phone
    +555133598017
    Email
    sfantin@hcpa.edu.br
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Carisi A Polanczyk
    Organizational Affiliation
    Federal University of Rio Grande do Sul - Faculty of Medicine
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Marco A Lumertz Saffi
    Organizational Affiliation
    Hospital de Clinicas de Porto Alegre
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Jeruza L Neyeloff
    Organizational Affiliation
    Hospital de Clinicas de Porto Alegre
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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